Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C1867132
Disease: Plantar crease between first and second toes
Plantar crease between first and second toes 		2 0 2 0.20 0 0
CUI: C4025806
Disease: High axial triradius
High axial triradius 		2 0 2 0.20 0 0
CUI: C4551859
Disease: RUBINSTEIN-TAYBI SYNDROME 1
RUBINSTEIN-TAYBI SYNDROME 1 		2 0 2 0.20 0 0
CUI: C1290508
Disease: Abnormal number of teeth
Abnormal number of teeth 		3 0 2 0.18 0 0
CUI: C4025111
Disease: Radial deviation of thumb terminal phalanx
Radial deviation of thumb terminal phalanx 		3 0 2 0.18 0 0
CUI: C0399357
Disease: Talon cusp
Talon cusp 		5 0 2 0.15 0 0
CUI: C0549397
Disease: Deviated nasal septum
Deviated nasal septum 		5 0 2 0.15 0 0
CUI: C0795940
Disease: Filippi syndrome
Filippi syndrome 		6 0 2 0.14 0 0
CUI: C1844508
Disease: Large foramen magnum
Large foramen magnum 		6 0 2 0.14 0 0
CUI: C1850327
Disease: Bifid uterus
Bifid uterus 		6 0 2 0.14 0 0
CUI: C1860164
Disease: Duplication of phalanx of hallux
Duplication of phalanx of hallux 		6 0 2 0.14 0 0
CUI: C4024221
Disease: Papillary cystadenoma of the epididymis
Papillary cystadenoma of the epididymis 		6 0 2 0.14 0 0
CUI: C0424304
Disease: Inappropriate laughter
Inappropriate laughter 		7 0 2 0.13 0 0
CUI: C0425772
Disease: Premature development of the breasts
Premature development of the breasts 		7 0 2 0.13 0 0
CUI: C0796022
Disease: Lujan Fryns syndrome
Lujan Fryns syndrome 		7 0 2 0.13 0 0
CUI: C1857627
Disease: Chorioretinal dystrophy
Chorioretinal dystrophy 		7 0 2 0.13 0 0
CUI: C1835807
Disease: Prominent fingertip pads
Prominent fingertip pads 		16 0 3 0.13 0 0
CUI: C0221214
Disease: Vascular ring
Vascular ring 		8 0 2 0.12 0 0
CUI: C0563243
Disease: Poor coordination
Poor coordination 		26 8 4 0.12 1 0.11
CUI: C2712334
Disease: Actual Aspiration
Actual Aspiration 		18 0 3 0.12 0 0
CUI: C1185616
Disease: Hair whorls
Hair whorls 		9 0 2 0.12 0 0
CUI: C1855670
Disease: Abnormal cornea morphology
Abnormal cornea morphology 		9 0 2 0.12 0 0
CUI: C0265372
Disease: Fetal hydantoin syndrome
Fetal hydantoin syndrome 		11 0 2 0.11 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 1.0E-01 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 1.0E-01 0 0